A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526511



Internal ID20899872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10020989..10023807hg38UCSC Ensembl
chr19:10131665..10134483hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382819
hg192819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044266
Samples
Known GenesRDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer